US2018296454A1PendingUtilityA1
Compositions for treating periodontitis and dental calculus accumulation
Assignee: UNIV NEW YORK STATE RES FOUNDPriority: May 5, 2016Filed: Jun 21, 2018Published: Oct 18, 2018
Est. expiryMay 5, 2036(~9.8 yrs left)· nominal 20-yr term from priority
A61K 9/0063A61Q 11/00A61K 8/44A61K 8/55A61K 8/602B64G 1/40A61K 2800/87A61K 2800/92A61K 8/732A61K 8/361B64G 1/64B64G 1/50B64G 1/407
64
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Compositions comprising serine and an organic mono- or multi-phosphate salt and methods of using such compositions to treat and/or prevent periodontal disease and/or dental calculus are provided.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating or preventing periodontitis and dental calculus accumulation, the method comprising administering to the oral environment of a subject, an effective amount of an oral composition comprising serine and at least one organic mono-phosphate or multi-phosphate salt.
2 . The method of claim 1 , wherein the composition further includes a buffer providing the composition with a pH of between about 6.1 and 7.0.
3 . The method of claim 2 , wherein the composition is provided as an orally acceptable dosage form, wherein the introduction of the composition to a subject suffering from periodontitis or dental calculus accumulation, reduces the alkalinity and thereby increases calcium concentration in the saliva by dissolving the calculus.
4 . The method of claim 2 , wherein the pH of the composition is between about 6.1 and about 6.3.
5 . The method of claim 2 , wherein the pH of the composition is between about 6.7 and about 7.0.
6 . The method of claim 1 , wherein the organic mono-phosphate or multi-phosphate salt is a biological salt.
7 . The method of claim 6 , wherein the biological salt is an inositol.
8 . The method of claim 7 , wherein the inositol is a phytate.
9 . The method of claim 8 , wherein the phytate is sodium phytate.
10 . The method of claim 3 , wherein the orally acceptable dosage form is selected from the group consisting of capsules, tablets, emulsions, aqueous suspensions, dispersions, pastes, powders, gums, and solutions.
11 . The method of claim 10 , wherein the orally acceptable dosage form comprises one or more carriers, one or more lubricating agents, or one or more diluents.
12 . The method of claim 11 , wherein the carrier is lactose or corn starch, the lubricating agent is magnesium stearate, and the diluent is lactose or dried corn starch.
13 . The method of claim 2 , wherein the orally acceptable dosage form comprises one or more sweetening, flavoring, or coloring agents.
14 . The method of claim 1 wherein the subject is at risk of developing plaque or periodontal disease.
15 . The method of claim 14 , wherein the subject is a human.
16 . The method of claim 15 , wherein the periodontal disease is gingivitis.
17 . The method of any of claim 1 , wherein the oral composition is applied to one or more teeth of the subject.
18 . The method of claim 17 , wherein the oral composition is applied to the enamel, exposed dentine, or cementum of one or more teeth of the subject.Join the waitlist — get patent alerts
Track US2018296454A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.